CASC15
cancer susceptibility 15
Summary
This gene produces a long non-coding RNA that may regulate cell proliferation. This RNA is upregulated in hepatocellular carcinoma, where it is thought to function as an oncogene. However, some splice variants of this gene may function as a tumor suppressor in neuroblastoma and other tumor types. Circular RNA variants were observed at this gene. [provided by RefSeq, Dec 2017]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs550140909 | 6:21,685,541 | G/C | — | — |
| rs6925119 | 6:21,701,083 | G/A | intron variant | — |
| rs116239840 | 6:21,722,970 | A/C | regulatory region variant | — |
| rs9460664 | 6:21,723,621 | G/A | intron variant | — |
| rs6926491 | 6:21,724,670 | G/A | intron variant | — |
| rs7772163 | 6:21,726,011 | G/C | intron variant | — |
| rs12213012 | 6:21,819,901 | G/T | — | — |
| rs142003747 | 6:21,822,215 | T/A | intron variant | — |
| rs1796683 | 6:21,835,946 | A/T | — | — |
| rs181230539 | 6:21,845,066 | C/G | intron variant | — |
| rs77634652 | 6:21,862,343 | G/A | — | — |
| rs11757605 | 6:21,888,181 | G/T | — | — |
| rs74971894 | 6:21,888,517 | A/C | — | — |
| rs12192041 | 6:21,924,904 | T/C | intron variant | — |
| rs28431967 | 6:21,926,992 | G/A | intron variant | — |
| rs17258904 | 6:21,928,131 | A/T | — | — |
| rs113219634 | 6:21,928,852 | C/T | intron variant | — |
| rs6938097 | 6:21,939,328 | G/A | intron variant | — |
| rs6909084 | 6:21,956,881 | C/A | intron variant | — |
| rs7763264 | 6:21,960,065 | C/T | intron variant | — |
| rs2078543 | 6:21,996,860 | A/G | intron variant | — |
| rs11966463 | 6:22,003,895 | A/C | regulatory region variant | — |
| rs13198656 | 6:22,004,909 | C/T | intron variant | — |
| rs1928168 | 6:22,017,738 | T/C | regulatory region variant | — |
| rs567753571 | 6:22,045,993 | C/T | — | — |
| rs55775505 | 6:22,057,566 | C/T | intron variant | — |
| rs4712651 | 6:22,062,485 | C/G | — | — |
| rs9460699 | 6:22,062,996 | T/C | — | — |
| rs4712652 | 6:22,078,615 | G/T | — | — |
| rs73389656 | 6:22,080,900 | G/T | upstream gene variant | — |
| rs16885582 | 6:22,095,606 | T/C | — | — |
| rs9358488 | 6:22,108,426 | C/T | intron variant | — |
| rs6905441 | 6:22,113,027 | T/C | regulatory region variant | — |
| rs4712653 | 6:22,125,964 | T/G | — | — |
| rs6899545 | 6:22,128,462 | C/T | — | — |
| rs9295536 | 6:22,131,929 | C/A | downstream gene variant | — |
| rs4712656 | 6:22,136,262 | G/C | coding sequence variant | — |
| rs9393235 | 6:22,139,634 | A/G | intron variant | — |
| rs6939340 | 6:22,140,004 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.